Primary Site >> Liver Cancer
Gene >> NRCAM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108178087:108178087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2877G>T |
| AA Mutation | p.Lys959Asn(p.K959N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108234650:108234650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.163G>C |
| AA Mutation | p.Asp55His(p.D55H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108166942:108166942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3445G>A |
| AA Mutation | p.Asp1149Asn(p.D1149N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108234658:108234658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155C>A |
| AA Mutation | p.Ser52Tyr(p.S52Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108168361:108168361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3229G>T |
| AA Mutation | p.Ala1077Ser(p.A1077S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379028 |
| Start | 108159521:108159521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3619C>T |
| AA Mutation | p.His1207Tyr(p.H1207Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379028 |
| Start | 108226290:108226290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758654630 |
| CDS Mutation | c.639C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |